Changing stroke rehab and research worldwide now.Time is Brain! trillions and trillions of neurons that DIE each day because there are NO effective hyperacute therapies besides tPA(only 12% effective). I have 523 posts on hyperacute therapy, enough for researchers to spend decades proving them out. These are my personal ideas and blog on stroke rehabilitation and stroke research. Do not attempt any of these without checking with your medical provider. Unless you join me in agitating, when you need these therapies they won't be there.

What this blog is for:

My blog is not to help survivors recover, it is to have the 10 million yearly stroke survivors light fires underneath their doctors, stroke hospitals and stroke researchers to get stroke solved. 100% recovery. The stroke medical world is completely failing at that goal, they don't even have it as a goal. Shortly after getting out of the hospital and getting NO information on the process or protocols of stroke rehabilitation and recovery I started searching on the internet and found that no other survivor received useful information. This is an attempt to cover all stroke rehabilitation information that should be readily available to survivors so they can talk with informed knowledge to their medical staff. It lays out what needs to be done to get stroke survivors closer to 100% recovery. It's quite disgusting that this information is not available from every stroke association and doctors group.

Monday, December 30, 2013

Computer chips with cell membranes may change how artificial organs and drugs are tested before they can be used on patients

And since we already can grow brains on a chip this style of testing might solve rodent model in inflammation is not the same as humans. At least that could be the case if we had a great stroke association directing where research should be going.
http://news.ubc.ca/2013/12/30/organs-on-a-chip-2/
Imagine if medical research and clinical drug tests could be done on artificially grown organs on microchips to save time, costs, and ease ethical concerns?
That’s the dream of James Feng, a professor in biological and chemical engineering at UBC.
“The potential is tremendous,” says Feng. “The main impact of organs grown this way will be on the design of drugs; the understanding of the pathological processes.”
Dr. Feng’s group carries out research in three broad areas: mechanics of biological cells and tissues, interfacial fluid dynamics, and mechanics and rheology of complex fluids.
The group has an inter-disciplinary flavour–crosscutting applied mathematics, cell biology, soft-matter physics and chemical and biomedical engineering—that is well-suited for exploring this burgeoning technology.
Implications for the pharmaceutical industry
Feng cites a Harvard study using a small silicon device that holds a thin layer of real cell membranes capable of producing motion similar to the heaving and breathing of a lung.
Organ models designed this way have the potential to be more accurate in drug and treatment trials, says Feng, as they can better mimic the functions of human organs, as opposed to animal models which are the current research standard.
“It’s more controlled and you can simplify the process much faster,” said Feng.
“Harvard researchers also injected drugs into their chip model to see how it changed its behaviour and to see the tissue’s reaction to mechanical or chemical disturbance,” he added.
“It’s very important for drug design and discovery and the pharmaceutical industry would be tremendously interested in that.”
In addition, organs on a chip present a less controversial option for organ model testing compared to stem cell research. According to Feng, this is because their ultimate goals are very different from each other.
“The research that tried to grow organs directly from stem cells is aiming for eventually implantable organs,” he said. “The idea of making the chip is to work toward replacing animal models, so as to be more accurate and realistic like human organs. While the ability to replicate a complex human organ function remains far off, the direction appeals to anyone who is hoping to reduce the use of animals in research.”
Simulating organ functions on a chip
Feng says this kind of organ testing offers the possibility of greatly reducing cost and time required for clinical trials.
“By using computer simulations we can generate results and insights, and run virtual tests much more easily and quickly,” he says.
“We can test maybe hundreds or thousands of designs of organ chips to be able to tell you whether you should try those ten designs instead of the hundreds one by one.”
Feng, who has a background in aerospace engineering, says this new bio-technology has the potential to transform the development of artificial organs and drugs the way computer simulations have replaced the use of wind tunnels for designing aircrafts.
“That used to be the dominant mode of designing crafts,” he said, “but that’s being replaced by online computer simulations because we understand the principles of aerodynamics so well.”
While UBC’s efforts in the field are in the early stages, Feng is reaching out to researchers from other backgrounds. He will be inviting leading scientists to UBC in July 2014 for a workshop that will centre on the growth of artificial organs and computer simulations. He is also exploring ideas of his own.
“I have a collaboration with an engineering colleague on how to use the microfluidic chip, the technology used to emulate the lung in the Harvard study, as a way of measuring malaria-infected red cells,” he said, suggesting that this is just one of the countless ways this new technology could be used to fuel future innovation.

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